Garrett's House is dedicated to the support, advice, and education of a genetic skin condition called Epidermolysis Bullosa or EB for short. Currently there is no cure or effective treatment for EB. Please take a moment to learn about EB, and how you can support others who struggle with EB everyday. Garrett's House also honors the memory of those who lost their brave fight against EB. Please check out the Garden of Angel to learn more about the precious butterfly angels.
Showing posts with label Baby Brody; recessive dystrophic epidermolysis bullosa. Show all posts
Showing posts with label Baby Brody; recessive dystrophic epidermolysis bullosa. Show all posts

February 3, 2012

EB in the News

 

S. Ind. 8-month-old continues to fight rare skin disease with help from community.  You can read about baby Brody here